Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Timur Selçuk Akpinar"'
Publikováno v:
Case Reports in Hematology, Vol 2015 (2015)
Multiple myeloma is a neoplastic plasma cell disorder. It is characterized by collections of abnormal plasma cells accumulating in the bone marrow, where they interfere with the production of normal blood cells. It usually presents as a multisystemic
Externí odkaz:
https://doaj.org/article/585fd5eeef3241ae9824ed2548a0e977
Autor:
Murat Aşık, Fatih Tufan, Timur Selçuk Akpınar, Nilgül Akalın, Elvan Ceyhan, Necmeddin Tunç, Zehra Işık Hasıloğlu, Mehmet Rıza Altıparmak, Tevfik Ecder, Sait Albayram
Publikováno v:
Balkan Medical Journal, Vol 33, Iss 6, Pp 652-656 (2016)
Background: There is sporadic data about the occurrence of spinal meningeal cysts in patients with autosomal dominant polycystic kidney disease (ADPKD). We suggest that there is a relationship with the frequency and size of spinal meningeal cysts and
Externí odkaz:
https://doaj.org/article/df715b37bdec4520a487da8dfefdb459
Autor:
Murat Kose, Samim Emet, Timur Selcuk Akpınar, Mehmet Ilhan, Ali Fuat Kaan Gok, Mubariz Dadashov, Tufan Tukek
Publikováno v:
Case Reports in Gastroenterology, Vol 9, Iss 2, Pp 152-155 (2015)
Orlistat is a pancreatic lipase inhibitor which is used to treat obesity. Due to the increasing prevalence of obesity, orlistat use is thought to rise progressively. We report an interesting case caused by orlistat use caught in the early stages of a
Externí odkaz:
https://doaj.org/article/74a06833dc2f46debc44723f40f5abac
Publikováno v:
Turkish Journal of Hematology, Vol 30, Iss 1, Pp 8-12 (2013)
OBJECTIVE: The MPL gene encodes the thrombopoietin receptor. Recently MPL mutations (MPL W515L or MPL W515K) were described in patients with essential thrombocythemia (ET) and primary (idiopathic) myelofibrosis (PMF). The prevalence and the clinical
Externí odkaz:
https://doaj.org/article/158ca4292e6b46ada24547765caf25dd
Publikováno v:
Case Reports in Cardiology, Vol 2015 (2015)
The aortopulmonary window (APW) is an abnormal communication between the ascending aorta and the pulmonary trunk in the presence of two separate semilunar valves. It is a rare congenital malformation which represents 0.1% of all congenital cardiac di
Externí odkaz:
https://doaj.org/article/4717d02f237340159ec048c1b9a23bf4